| scholarly article | Q13442814 |
| P50 | author | Soeren S Lienkamp | Q55711745 |
| Albrecht Kramer-Zucker | Q65088047 | ||
| Jeroen van Reeuwijk | Q85313594 | ||
| Troels Ring | Q92136688 | ||
| Sophie Saunier | Q28322375 | ||
| Marius Ueffing | Q28323182 | ||
| Edgar A. Otto | Q30348357 | ||
| Florian Grahammer | Q38291359 | ||
| Mogens Vyberg | Q38326517 | ||
| Neil J. Sebire | Q38549176 | ||
| P2093 | author name string | Friedhelm Hildebrandt | |
| Gerd Walz | |||
| Karsten Boldt | |||
| Lars Pape | |||
| Ronald Roepman | |||
| Takayuki Yasunaga | |||
| Emilie Filhol | |||
| Jan Halbritter | |||
| Carsten Bergmann | |||
| Tobias B Huber | |||
| E Wolfgang Kuehn | |||
| Peter C Harris | |||
| Hanno J Bolz | |||
| Tobias Eisenberger | |||
| Søren Rittig | |||
| Thomas J Neuhaus | |||
| Joanna A E van Wijk | |||
| Detlef Bockenhauer | |||
| Sylvia Hoff | |||
| Mariet W Elting | |||
| Martin Pohl | |||
| Valeska Frank | |||
| Martin Helmstädter | |||
| Christopher Boehlke | |||
| Daniel Epting | |||
| Nicola Horn | |||
| Christoph Schell | |||
| Neveen A Soliman Elshakhs | |||
| Thanh-Minh T Nguyen | |||
| Sarah J Koon | |||
| Miriam Mergen | |||
| P2860 | cites work | A novel tandem affinity purification strategy for the efficient isolation and characterisation of native protein complexes | Q24299311 |
| Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy | Q24300810 | ||
| Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways | Q24302034 | ||
| NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis | Q24306642 | ||
| Localization of Inv in a distinctive intraciliary compartment requires the C-terminal ninein-homolog-containing region. | Q51945543 | ||
| Mutations of NPHP2 and NPHP3 in infantile nephronophthisis | Q57955396 | ||
| Experimental Protein Mixture for Validating Tandem Mass Spectral Analysis | Q59591383 | ||
| The role of Xenopus frizzled-8 in pronephric development | Q80546312 | ||
| VEGF receptor inhibition slows the progression of polycystic kidney disease | Q81326073 | ||
| Factor inhibiting HIF limits the expression of hypoxia-inducible genes in podocytes and distal tubular cells | Q84764376 | ||
| Nephrocystin-3 is required for ciliary function in zebrafish embryos | Q24312027 | ||
| Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia | Q24315070 | ||
| MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis | Q28000044 | ||
| A statistical model for identifying proteins by tandem mass spectrometry | Q28186251 | ||
| Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia | Q28585433 | ||
| The ciliary protein Nek8/Nphp9 acts downstream of Inv/Nphp2 during pronephros morphogenesis and left-right establishment in zebrafish | Q28586620 | ||
| Ciliopathies | Q29614821 | ||
| Regulation of ciliary polarity by the APC/C. | Q30491092 | ||
| Inversin relays Frizzled-8 signals to promote proximal pronephros development | Q30497559 | ||
| Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies | Q33682550 | ||
| Nephronophthisis-associated ciliopathies | Q34629900 | ||
| Involvement of hypoxia-inducible transcription factors in polycystic kidney disease | Q35781329 | ||
| Factor inhibiting HIF (FIH) recognizes distinct molecular features within hypoxia-inducible factor-α (HIF-α) versus ankyrin repeat substrates | Q35841949 | ||
| Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros. | Q35990548 | ||
| Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy | Q36277070 | ||
| Clinical spectrum and pathogenesis of nephronophthisis | Q37990376 | ||
| The Rac1 regulator ELMO1 controls vascular morphogenesis in zebrafish. | Q39704181 | ||
| Tandem affinity purification of ciliopathy-associated protein complexes | Q39900302 | ||
| Missense mutation in sterile alpha motif of novel protein SamCystin is associated with polycystic kidney disease in (cy/+) rat. | Q46738223 | ||
| The Wilms tumor genes wt1a and wt1b control different steps during formation of the zebrafish pronephros. | Q47073608 | ||
| A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish | Q47073857 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Ankyrin repeat and sterile alpha motif domain containing 6 | Q29821651 |
| NIMA-related kinase 8 | Q29834830 | ||
| Nephronophthisis 3 | Q29835864 | ||
| P304 | page(s) | 951-956 | |
| P577 | publication date | 2013-06-23 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3 | |
| P478 | volume | 45 |
| Q38851585 | A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling |
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| Q27321009 | ANKS3 Co-Localises with ANKS6 in Mouse Renal Cilia and Is Associated with Vasopressin Signaling and Apoptosis In Vivo in Mice |
| Q48159062 | ANKS3 is mutated in a family with autosomal recessive laterality defect |
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| Q35554078 | An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease |
| Q28578791 | Anks3 interacts with nephronophthisis proteins and is required for normal renal development |
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| Q52844921 | From fish to nephrology: modelling glomerular function in Danio rerio larvae. |
| Q33728229 | From the cytoplasm into the cilium: bon voyage |
| Q40472297 | GTP-binding of ARL-3 is activated by ARL-13 as a GEF and stabilized by UNC-119. |
| Q90669133 | Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association |
| Q38563680 | Genetic basis of human left-right asymmetry disorders |
| Q36719160 | Genetic link between renal birth defects and congenital heart disease |
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| Q91272233 | Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer's disease |
| Q27316952 | Global genetic analysis in mice unveils central role for cilia in congenital heart disease |
| Q37289871 | High-resolution genetic localization of a modifying locus affecting disease severity in the juvenile cystic kidneys (jck) mouse model of polycystic kidney disease |
| Q35610258 | In vivo investigation of cilia structure and function using Xenopus |
| Q51799948 | Influence of the R823W mutation on the interaction of the ANKS6-ANKS3: insights from molecular dynamics simulation and free energy analysis. |
| Q48045737 | Intracellular calcium increases in vascular smooth muscle cells with progression of chronic kidney disease in a rat model |
| Q57200216 | Is ciliary Hedgehog signalling dispensable in the kidneys? |
| Q36026246 | Lack of Benefit of Early Intervention with Dietary Flax and Fish Oil and Soy Protein in Orthologous Rodent Models of Human Hereditary Polycystic Kidney Disease |
| Q101141425 | Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome |
| Q47833085 | Many Genes-One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders. |
| Q94600217 | Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes |
| Q55563743 | Metabolic Phenotyping of Anks3 Depletion in mIMCD-3 cells - a Putative Nephronophthisis Candidate. |
| Q64062735 | Modeling congenital kidney diseases in |
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| Q33974574 | Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD. |
| Q32884490 | Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease. |
| Q87248470 | Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies |
| Q47974544 | Mutations in the Katnb1 gene cause left-right asymmetry and heart defects |
| Q90280361 | NPHP proteins are binding partners of nucleoporins at the base of the primary cilium |
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